Pembrolizumab versus placebo as adjuvant therapy in resected stage IIB or IIC melanoma: Outcomes in histopathologic subgroups from the randomized, double-blind, phase 3 KEYNOTE-716 trial

BackgroundAdjuvant pembrolizumab significantly improved recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) versus placebo in the phase 3 KEYNOTE-716 study of resected stage IIB or IIC melanoma. At the prespecified third interim analysis (data cut-off, January 4, 2022), the HR...

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Veröffentlicht in:Journal for immunotherapy of cancer 2024-03, Vol.12 (3), p.e007501
Hauptverfasser: Schadendorf, Dirk, Luke, Jason John, Ascierto, Paolo A, Long, Georgina V, Rutkowski, Piotr, Khattak, Adnan, Del Vecchio, Michele, de la Cruz-Merino, Luis, Mackiewicz, Jacek, Sileni, Vanna Chiarion, Kirkwood, John M, Robert, Caroline, Grob, Jean-Jacques, Dummer, Reinhard, Carlino, Matteo S, Zhao, Yujie, Kalabis, Mizuho, Krepler, Clemens, Eggermont, Alexander, Scolyer, Richard A
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Sprache:eng
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Zusammenfassung:BackgroundAdjuvant pembrolizumab significantly improved recurrence-free survival (RFS) and distant metastasis-free survival (DMFS) versus placebo in the phase 3 KEYNOTE-716 study of resected stage IIB or IIC melanoma. At the prespecified third interim analysis (data cut-off, January 4, 2022), the HR for RFS in the overall population was 0.64 (95% CI, 0.50 to 0.84) and the HR for DMFS was 0.64 (95% CI, 0.47 to 0.88). We present a post hoc analysis of efficacy by subtypes defined by histopathologic characteristics.MethodsPatients aged ≥12 years with newly diagnosed, resected stage IIB or IIC melanoma were randomly assigned (1:1) to pembrolizumab 200 mg every 3 weeks (2 mg/kg up to 200 mg for pediatric patients) or placebo. The primary end point was RFS per investigator review; DMFS per investigator review was secondary. Subgroups of interest were melanoma subtype (nodular vs non-nodular), tumor thickness (≤4 mm vs >4 mm), presence of ulceration (yes vs no), mitotic rate (4 mm; 0.66 (0.50 to 0.89) for ulceration and 0.57 (0.32 to 1.03) for no ulceration; 0.57 (0.35 to 0.92) for mitotic rate
ISSN:2051-1426
2051-1426
DOI:10.1136/jitc-2023-007501